A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5452285



Internal ID230444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:215625375..215625487hg38UCSC Ensembl
chr1:215798717..215798829hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16896682
Samples
Known GenesUSH2A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5452285
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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